Further evidence for genetic heterogeneity of autosomal dominant disorders with accumulation of multiple deletions of mitochondrial DNA
Author:
Publisher
BMJ
Subject
Genetics(clinical),Genetics
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. POS5 Gene of Saccharomyces cerevisiae Encodes a Mitochondrial NADH Kinase Required for Stability of Mitochondrial DNA;Eukaryotic Cell;2003-08
2. Progressive External Ophthalmoplegia Characterized by Multiple Deletions of Mitochondrial DNA: Unraveling the Pathogenesis of Human Mitochondrial DNA Instability and the Initiation of a Genetic Classification;NeuroMolecular Medicine;2003
3. Active Site Mutation in DNA Polymerase γ Associated with Progressive External Ophthalmoplegia Causes Error-prone DNA Synthesis;Journal of Biological Chemistry;2002-05
4. Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions;Nature Genetics;2001-07
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